The effects of the magnesium doping of binary glass (Si–Ca) on particle texture, on the biomineralization process in simulated body fluid (SBF) as well as on drug loading and release were examined. For this purpose, magnesium-doped binary bioglass nanoparticles (85SiO₂–(15 − x)CaO–xMgO, with x = 1, 3, 5 and 10 mol%) were prepared by a base catalysed sol–gel method. N₂ adsorption isotherm analysis showed an enhancement in specific surface area as the Mg molar fraction increased. In addition, the FTIR spectra of the samples after soaking in SBF for various periods of time confirmed the presence of new chemical bonds related to the apatite phase, as was also confirmed by SEM observations. XRD patterns of the samples after soaking revealed that the crystallization to form a more stable apatite-like phase was hindered with increasing magnesium content in the glass composition. Furthermore, it was proved that the kinetics of drug release improved with increasing magnesium content. The porosity and the specific surface area were found to be responsible for this improvement.

The electron transfer dynamics and electrocatalytic behaviour of ferrocene-terminated self-assembled monolayers (SAMs), co-adsorbed with single-walled carbon nanotubes (SWCNTs) on a gold electrode, have been interrogated for the first time. Ferrocene monocarboxylic acid (FMCA) or ferrocene dicarboxylic acid (FDCA) was covalently attached to the cysteamine (Cys) monolayer to form Au-Cys-FMCA and Au-Cys-FDCA, respectively. The same covalent attachment strategy was used to form the mixed SWCNTs and ferrocene-terminated layers (i.e. Au-Cys-SWCNT/FMCA and Au-Cys-SWCNT/FDCA). Using cyclic voltammetry and electrochemical impedance spectroscopy, the impact of neighbouring SWCNTs on the electron transfer dynamics of the ferrocene molecular assemblies in an acidic medium (0.5 M H₂SO₄) and in a solution of an outer-sphere redox probe ([Fe(CN)₆]^{4 −}/[Fe(CN)₆]^{3 −}) was explored. The electron transfer rate constants in both media essentially decreased as Au-Cys-FMCA > Au-Cys-SWCNT/FDCA > Au-Cys-FDCA > Au-Cys-SWCNT/FMCA. This trend has been interpreted in terms of several factors such as the locations of the ferrocene species in a range of environments with a range of potentials, the proximity/interactions of the ferrocenes with one another, and electrostatic interaction or repulsion existing between the negatively-charged redox probe and the modified electrodes. The thiocyanate ion (SCN ⁻) was used as a model analyte to examine the influence of the neighbouring SWCNTs on the electrocatalytic ability of the ferrocene assemblies. The Au-Cys-SWCNT/FDCA showed the best catalytic activity (in terms of onset potential and catalytic peak current height) for the oxidation of SCN ⁻, possibly due to the repulsive interactions between the negatively charged SCN ⁻ and high number of surface –COOH species at the SWCNT/FDCA. This study has provided some useful insights as to how CNTs co-assembled with ferrocene-terminated thiols could impact on the electron transfer kinetics as well as the electrocatalytic detection of the self-assembled ferrocene layers.

Photoinduced second harmonic generation (SHG) in Au nanoparticle-deposited ZnO nanocrystallite (NC) films was explored by applying bicolor coherent treatment of a Nd-YAG laser with wavelength 1.06 µm and its SHG. We have established that coexistence of the ZnO and Au nanoparticles gives a substantially larger SHG output with respect to pure ZnO NC deposited on the glass substrate. It was established that the value of the second order susceptibility is about 23 pm V(-1). Better nonlinear optical susceptibilities were obtained during phototreatment at temperatures near 30-35 °C for the Au doped samples. The samples without gold NCs are temperature independent. Generally an increasing temperature leads to a decrease of the optical SHG.